Targeted and highly efficient gene transfer into CD4+ cells by a recombinant human immunodeficiency virus retroviral vector.

Ítems similars

• High-efficiency gene transfer into CD34+ cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G.
  per: Akkina, R K, et al.
  Publicat: (1996)
• Targeted inhibition of immunodeficiency virus replication in lymphocytes through retroviral mediated gene transfer
  per: Tung, F. Y. -T., et al.
  Publicat: (1993)
• Retroviral Vector Targeting to Human Immunodeficiency Virus Type 1-Infected Cells by Receptor Pseudotyping
  per: Somia, Nikunj V., et al.
  Publicat: (2000)
• Highly Efficient and Selective CAR-Gene Transfer Using CD4- and CD8-Targeted Lentiviral Vectors
  per: Jamali, Arezoo, et al.
  Publicat: (2019)
• CD4-Negative Cells Bind Human Immunodeficiency Virus Type 1 and Efficiently Transfer Virus to T Cells
  per: Olinger, Gene G., et al.
  Publicat: (2000)